Canonical Allele Identifier: PA2826957989
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 570104
ClinVar RCV Id: RCV000991793 RCV002315991 RCV000690891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Pro558Ala
CA4759546
NM_001316690.1:c.1672C>G